Compound Identification
SMILES
CCCCCCCCCCCCCCCCCCCCCCCCCC(=O)NC(CS[C@H]1OC(CO)[C@H](O)C(O)C1O)C(O)C(O)CCCCCCCCCCCCCC
InChIKey
InChIKey=QJZCEVLGGRYOKC-QJRSUPKLSA-N
Formula
C50H99NO8S
Mass
874.4
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Lipids and lipid-like molecules
-
Class
Sphingolipids
- Subclass Glycosphingolipids
-
Class
Sphingolipids
-
Superclass
Lipids and lipid-like molecules
Kingdom
Organic compounds
Superclass
Lipids and lipid-like molecules
Class
Sphingolipids
Subclass
Glycosphingolipids
Intermediate Tree Nodes
Not available
Direct Parent
Glycosphingolipids
Alternative Parents
Hexoses Thioglycosides Oxanes N-acyl amines Monothioacetals Secondary carboxylic acid amides Secondary alcohols Sulfenyl compounds Polyols Oxacyclic compounds Primary alcohols Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aliphatic heteromonocyclic compounds
Substituents
Glycosphingolipid - Hexose monosaccharide - Glycosyl compound - S-glycosyl compound - Fatty amide - Monosaccharide - N-acyl-amine - Oxane - Fatty acyl - Monothioacetal - Secondary carboxylic acid amide - Secondary alcohol - Carboxamide group - Oxacycle - Carboxylic acid derivative - Polyol - Organoheterocyclic compound - Sulfenyl compound - Organic oxide - Carbonyl group - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Alcohol - Hydrocarbon derivative - Organooxygen compound - Organosulfur compound - Primary alcohol - Aliphatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as glycosphingolipids. These are sphingolipids containing a saccharide moiety glycosidically attached to the sphingoid base. Although saccharide moieties are mostly O-glycosidically linked to the ceramide moiety, other sphingolipids with glycosidic bonds of other types (e.g. S-,C-, or N-type) has been reported.
External Descriptors
Not available